Canonical Allele Identifier: PA132045
Gene: MYH7 HGNC NCBI

Linked Data

ClinVar Variation Id: 43044
ClinVar RCV Id: RCV000035938 RCV000148696 RCV000465008 RCV000620929 RCV000758026 RCV000989185 RCV000853439 RCV002227441 RCV001703873 RCV004541080
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000248.2:p.Ala1637Thr
CA015454
NM_000257.4:c.4909G>A